Ihara Medics U.S., Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ketorex Sanwa Standards Ref K903365
Regimes: 510(k) Registry: 510(k)Ketorex C Sanwa Ref K953452
Regimes: 510(k) Registry: 510(k)Ketone Test B Sanwa Standard Ref K903366
Regimes: 510(k) Registry: 510(k)Keto-340 Ii Ref K912373
Regimes: 510(k) Registry: 510(k)Ketone Test A Sanwa Standard Ref K903367
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ihara Medics U.S., Inc. have in the registry?
The registry currently lists 5 devices for Ihara Medics U.S., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ihara Medics U.S., Inc.'s devices?
Among its 5 most recently registered devices, Ihara Medics U.S., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Ihara Medics U.S., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Ihara Medics U.S., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ihara Medics U.S., Inc. in the registry?
The most recently registered devices listed for Ihara Medics U.S., Inc. include KETOREX SANWA STANDARDS, KETOREX C SANWA, KETONE TEST B SANWA STANDARD and KETO-340 II.